Evidence map›Paper›PMID 42683345›Full record

ArticleInternational journal of sexual health : official journal of the World Association for Sexual Health2026

FULLSENSE-An Online Intervention Program for Adults Reporting Sexual Difficulties: A Two-Armed Randomized Controlled Pilot Trial Protocol.

Ana Rita Barros, Priscila A Vasconcelos, Ana Luísa Quinta Gomes, Mariana Carrito, Ana Luísa Patrão, Leonor de Oliveira, Sandra Aguiar, Joana Carvalho, Pedro J Nobre

Abstract read
In one paragraph

Article in International journal of sexual health : official journal of the World Association for Sexual Health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Ana Rita BarrosCenter for Psychology, University of Porto, Porto, Portugal.ORCID https://orcid.org/0009-0006-7685-9462
Priscila A VasconcelosCenter for Psychology, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-0161-0682
Ana Luísa Quinta GomesCenter for Psychology, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-6421-656X
Mariana CarritoCenter for Psychology, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0001-8414-5319
Ana Luísa PatrãoCenter for Psychology, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-2027-5461
Leonor de OliveiraCenter for Psychology, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-9903-8046
Sandra AguiarCenter for Psychology, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0001-6500-9039
Joana CarvalhoWilliam James Center for Research, Departamento de Educação e Psicologia, Universidade de Aveiro, Aveiro, Portugal.ORCID https://orcid.org/0000-0003-2362-0010
Pedro J NobreCenter for Psychology, University of Porto, Porto, Portugal.ORCID https://orcid.org/0000-0003-2571-6972

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sexuality is a key aspect of human life, significantly influencing health, well-being, and quality of life. Sexual dysfunction may occur throughout the sexual response cycle and is commonly associated with psychological distress and dissatisfaction. Online interventions have proven effective in promoting sexual health by providing accessible, private, and evidence-based support. Cognitive-behavioral therapy (CBT) and mindfulness-based methods show promise in treating sexual dysfunction, enhancing function, increasing satisfaction, and reducing distress. Embracing a comprehensive and positive, pleasure-inclusive view of sexuality is vital for supporting sexual health and overall well-being. This study presents the protocol for a feasibility pilot randomized controlled trial evaluating FULLSENSE, an 8-week, guided online intervention designed to improve sexual well-being in adults reporting sexual dysfunction. Methods: A two-arm, parallel, open-label design, with the waiting-list control group receiving treatment as usual will be conducted. Participants (N = 70) meeting eligibility criteria will be randomly assigned to the FULLSENSE intervention or a waiting-list control group. Primary outcomes will assess the intervention's acceptability, usability, and feasibility. Secondary outcomes will evaluate preliminary efficacy in improving sexual satisfaction, functioning, pleasure, and reducing sexual distress, while cognitive and neurophysiological assessments will allow us to explore functional connectivity and correlates of implicit cognition and interoception. Data collection will include self-reported measures and neurophysiology assessments for a nested sample. Results: Findings will provide insights into the feasibility and preliminary efficacy of FULLSENSE, informing future large-scale trials. If successful, this intervention may facilitate access to sexual health care and support individuals experiencing sexual distress. Conclusion: The FULLSENSE feasibility pilot trial promises valuable insights into an accessible, evidence-based online intervention for sexual dysfunction, potentially contributing to digital sexual health solutions. The findings of the forthcoming studies will support the intervention's implementation and ultimately facilitate sexual healthcare access and support.

Indexed as

feasibility studyonline interventionrandomized controlled trialsexual dysfunctionsSexual health

Identifiers

PMID42683345
PMCPMC13531999

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.